Cleared Traditional

K062069 - ATLANTIS ABUTMENT FOR 3I MICROMINI IMPLANT

K062069 is an FDA 510(k) clearance for ATLANTIS ABUTMENT FOR 3I MICROMINI IMPLANT, manufactured by Atlantis Components, Inc.. The device is a Class 2 Dental device with product code NHA cleared through the Traditional 510(k) pathway after a 208-day FDA review.

K062069 · Atlantis Components, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 2007
Decision
208d
Days
Class 2
Risk

K062069 is an FDA 510(k) clearance for the ATLANTIS ABUTMENT FOR 3I MICROMINI IMPLANT. Classified as Abutment, Implant, Dental, Endosseous within the NHA classification (a category for dental implant abutments and prosthetic components), Class II - Special Controls.

Submitted by Atlantis Components, Inc. (Skokie, US). The FDA issued a Cleared decision on February 14, 2007 after a review of 208 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3630 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Atlantis Components, Inc. devices

FDA 510(k) Submission Details - K062069

510(k) Number K062069 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 21, 2006
Decision Date February 14, 2007
Days to Decision 208 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
81d slower than avg
Panel avg: 127d · This submission: 208d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NHA Device Classification - Class 2, Special Controls

Product Code NHA Abutment, Implant, Dental, Endosseous
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3630
Definition To Be Used In Conjunction With An Endosseous Dental Implant Fixture To Aid In Prosthetic Rehabilitation.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Dental devices follow this clearance model.

Regulatory Peers - NHA Abutment, Implant, Dental, Endosseous

All 558
Devices cleared under the same product code (NHA) and FDA review panel - the closest regulatory comparables to K062069.
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